<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klementyeva SV</submitter><funding>Klaus Tschira Foundation</funding><pagination>1994</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9965685</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(4)</volume><pubmed_abstract>We report the synthesis and characterization of two types of new mixed-ligand rare earth complexes: tetracoordinate (NacNac&lt;sup>Mes&lt;/sup>)Ln(BIAN&lt;sup>dipp&lt;/sup>) (Ln = Dy (&lt;b>1&lt;/b>), Er (&lt;b>2&lt;/b>) and Y (&lt;b>3&lt;/b>)) and pentacoordinate (NacNac&lt;sup>Mes&lt;/sup>)Ln(AP&lt;sup>dipp&lt;/sup>)(THF) (Ln = Dy (&lt;b>4&lt;/b>), Er (&lt;b>5&lt;/b>) and Y (&lt;b>6&lt;/b>)). The first three compounds were prepared by the reaction of [(BIAN&lt;sup>Dipp&lt;/sup>)LnI] with potassium β-diketiminate. The salt metathesis of β-diketiminato-supported rare earth dichlorides (NacNac&lt;sup>Mes&lt;/sup>)LnCl&lt;sub>2&lt;/sub>(THF)&lt;sub>2&lt;/sub> with sodium o-amidophenolate results in compounds &lt;b>4&lt;/b>-&lt;b>6&lt;/b>. The crystal structures of complexes &lt;b>1&lt;/b>-&lt;b>6&lt;/b> were determined by single-crystal analysis. The combination of bulky monoanionic N-mesityl-substituted β-diketiminates with sterically hindered redox-active ligands led to the very low coordination numbers of rare earths and strong distortion of the chelate ligands.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Low-Coordinate Mixed Ligand NacNac Complexes of Rare Earth Metals.</pubmed_title><pmcid>PMC9965685</pmcid><funding_grant_id>project GSO/KT37</funding_grant_id><pubmed_authors>Abramov PA</pubmed_authors><pubmed_authors>Poddel'sky AI</pubmed_authors><pubmed_authors>Sukhikh TS</pubmed_authors><pubmed_authors>Klementyeva SV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low-Coordinate Mixed Ligand NacNac Complexes of Rare Earth Metals.</name><description>We report the synthesis and characterization of two types of new mixed-ligand rare earth complexes: tetracoordinate (NacNac&lt;sup>Mes&lt;/sup>)Ln(BIAN&lt;sup>dipp&lt;/sup>) (Ln = Dy (&lt;b>1&lt;/b>), Er (&lt;b>2&lt;/b>) and Y (&lt;b>3&lt;/b>)) and pentacoordinate (NacNac&lt;sup>Mes&lt;/sup>)Ln(AP&lt;sup>dipp&lt;/sup>)(THF) (Ln = Dy (&lt;b>4&lt;/b>), Er (&lt;b>5&lt;/b>) and Y (&lt;b>6&lt;/b>)). The first three compounds were prepared by the reaction of [(BIAN&lt;sup>Dipp&lt;/sup>)LnI] with potassium β-diketiminate. The salt metathesis of β-diketiminato-supported rare earth dichlorides (NacNac&lt;sup>Mes&lt;/sup>)LnCl&lt;sub>2&lt;/sub>(THF)&lt;sub>2&lt;/sub> with sodium o-amidophenolate results in compounds &lt;b>4&lt;/b>-&lt;b>6&lt;/b>. The crystal structures of complexes &lt;b>1&lt;/b>-&lt;b>6&lt;/b> were determined by single-crystal analysis. The combination of bulky monoanionic N-mesityl-substituted β-diketiminates with sterically hindered redox-active ligands led to the very low coordination numbers of rare earths and strong distortion of the chelate ligands.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-19T07:37:48.621Z</modification><creation>2025-02-18T23:57:49.564Z</creation></dates><accession>S-EPMC9965685</accession><cross_references><pubmed>36838980</pubmed><doi>10.3390/molecules28041994</doi></cross_references></HashMap>